男性神经性厌食症与DNA甲基化改变有关

Artem Kim, B. Izac, N. Lebrun, N. Ramoz, C. Blanchet, F. Letourneur, M. Moro, P. Gorwood, M. Tayrac, T. Bienvenu
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摘要

目的:神经性厌食症(Anorexia nervosa, AN)是一种严重的精神疾病,以异常的饮食行为为特征,导致体重下降和死亡率增加。虽然在女性中更为常见,但估计5%至10%的受影响患者是男性。到目前为止,男性AN的确切病因尚不清楚。与许多精神疾病一样,这可能是遗传、生物、心理和环境因素的综合作用。在这里,我们使用全基因组亚硫酸盐测序来确定AN男性个体的甲基组。方法:我们对6例AN限制性型男性患者的3,340,894个生物相关CpG位点(Illumina TruSeqMethyl Capture EPIC试剂盒)进行亚硫酸盐测序分析。为了减少环境影响,选取4个相关的未受影响的个体作为对照。结果:在AN限制性型男性患者与未受影响的对照组的比较中,发现153个差异甲基化区域和1812个差异甲基化的CpGs,对应于与代谢和营养状况、精神状态和免疫功能相关的基因。此外,String网络分析软件还发现了一个与MAPK信号通路、PI3K-Akt信号通路和神经营养因子信号通路相关的子网络。结论:我们的研究结果重复了之前在女性AN中发现的几个靶基因,如PRKAG2、RPTOR和ICAM5,并发现了新的信号通路,包括PI3K-Akt和神经营养因子信号通路在AN中受到干扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Altered DNA methylation associated with nervosa anorexia in males
Purpose: Anorexia nervosa (AN) is a serious psychiatric disorder characterized by abnormal eating behaviors, resulting in weight loss and increased mortality. Although more common in females, an estimated 5 to 10% of affected patients are males. Up to now, the exact cause of male AN is unknown. As with many psychiatric diseases, it's probably a combination of genetic, biological, psychological and environmental factors. Here, we used whole-genome bisulfite sequencing to determine the methylome of male individuals with AN. Methods: We analyzed by bisulfite sequencing 3,340,894 biologically relevant CpG sites (Illumina TruSeqMethyl Capture EPIC kit) of 6 male patients affected with AN restrictive type. To reduce the environment effect, 4 related unaffected individuals were selected as controls. Results: Comparisons between male patients affected with AN restrictive type and unaffected controls showed 153 differentially methylated regions and 1812 differentially methylated CpGs that corresponded to genes relevant to metabolic and nutritional status, psychiatric status and immune function. Moreover, the String network analysis software identified a subnetwork, related to MAPK signaling pathway, PI3K-Akt signaling pathway and neurotrophin signaling pathway. Conclusions: Our findings replicate several results concerning several target genes such as PRKAG2, RPTOR, and ICAM5 previously identified in female AN, and identified novel signaling pathways involving PI3K-Akt and neurotrophin signaling pathway disturbed in AN.
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